Department of Pathology, UMass Medical School, Worcester, MA, United States.
Front Immunol. 2021 Mar 9;12:636568. doi: 10.3389/fimmu.2021.636568. eCollection 2021.
Major histocompatibility class I (MHC I) molecules bind peptides derived from a cell's expressed genes and then transport and display this antigenic information on the cell surface. This allows CD8 T cells to identify pathological cells that are synthesizing abnormal proteins, such as cancers that are expressing mutated proteins. In order for many cancers to arise and progress, they need to evolve mechanisms to avoid elimination by CD8 T cells. MHC I molecules are not essential for cell survival and therefore one mechanism by which cancers can evade immune control is by losing MHC I antigen presentation machinery (APM). Not only will this impair the ability of natural immune responses to control cancers, but also frustrate immunotherapies that work by re-invigorating anti-tumor CD8 T cells, such as checkpoint blockade. Here we review the evidence that loss of MHC I antigen presentation is a frequent occurrence in many cancers. We discuss new insights into some common underlying mechanisms through which some cancers inactivate the MHC I pathway and consider some possible strategies to overcome this limitation in ways that could restore immune control of tumors and improve immunotherapy.
主要组织相容性复合体 I (MHC I) 分子结合来自细胞表达基因的肽段,然后将这种抗原信息运输并呈现在细胞表面。这使得 CD8 T 细胞能够识别合成异常蛋白的病理性细胞,例如表达突变蛋白的癌症。为了让许多癌症发生和发展,它们需要进化出机制来避免被 CD8 T 细胞消除。MHC I 分子对于细胞存活不是必需的,因此癌症逃避免疫控制的一种机制是失去 MHC I 抗原呈递机制 (APM)。这不仅会削弱自然免疫反应控制癌症的能力,也会挫败通过重新激活抗肿瘤 CD8 T 细胞(如检查点阻断)发挥作用的免疫疗法。在这里,我们回顾了大量证据,证明 MHC I 抗原呈递的丧失在许多癌症中经常发生。我们讨论了一些常见的潜在机制的新见解,这些机制使一些癌症失活 MHC I 途径,并考虑了一些可能的策略来克服这种限制,从而恢复对肿瘤的免疫控制并改善免疫治疗。